Mutant Glucose Dehydrogenase

ABSTRACT

Substrate specificity for glucose of a glucose dehydrogenase having the amino acid sequence of SEQ ID NO: 13 is improved by substituting another amino acid residue for the amino acid residue at position 472 and/or 475.

TECHNICAL FIELD

The present invention relates to a mutant glucose dehydrogenase showing improved substrate specificity. The mutant glucose dehydrogenase of the present invention can be suitably used for glucose sensors, glucose assay kits and so forth, and is useful in the fields of biochemistry, clinical medicine, and so forth.

BACKGROUND ART

In recent years, a variety of enzymes are used as biosensor elements. Glucose oxidases (GODs) have already been practically used as sensor elements for measuring blood glucose levels for the purpose of diagnosis of diabetes. However, GODs suffer from a problem that they are affected by dissolved oxygen in samples. Therefore, glucose dehydrogenases (GDHs), which are not affected by dissolved oxygen in samples, are drawing attentions as alternatives of GODs.

As GDHs, one requiring NAD(P)⁺ as a coenzyme (E.C.1.1.1.47), one requiring pyroloquinoline quinone (PQQ) as a coenzyme (PQQGDH; E.C.1.1.99.17) etc. have been reported. GDH requiring NAD(P)⁺ as a coenzyme suffers from a problem as a sensor element that NAD(P)⁺ needs to be added to the assay system. On the other hand, it is unnecessary for coenzyme-binding type GDHs such as PQQGDH to add a coenzyme to the assay system.

Further, sensor elements are desired to exhibit a stability that the function as a sensor is not lost even when they are continuously used or left at room temperature.

Since enzymes derived from thermophilic bacteria which grow at high temperature generally exhibit high thermostability, and high stability even in long-term storage, continuous use and so forth, application of them as sensor elements is expected. However, although GDHs derived from Thermoplasma acidophilum and Sulfolobus solfataricus have been reported as thermostable GDHs derived from thermophilic bacteria, both of them require NAD(P)⁺ as a coenzyme.

On the other hand, thermostable GDH produced by Burkholderia cepacia, a moderately thermophilic bacterium, is an FAD-binding type GDH, and the enzymological characteristics thereof such as optimum reaction temperature, thermostability and substrate specificity have already been elucidated (Patent document 1). This GDH usually exists as a heterooligomer consisting of a catalytic subunit (α-subunit) showing high heat resistance, an electron transfer subunit (β-subunit), which is cytochrome C, and γ-subunit of which function is unknown, and its optimum reaction temperature is 45° C. These subunits are dissociated by a heat treatment at a temperature higher than 50° C. to release the α-subunit monomer of which optimum reaction temperature is 75° C. The α-subunit monomer is thermostable and exhibits 80% or more of residual activity even after a heat treatment at 60° C. for 30 minutes. The genes coding for these subunits have also already been isolated (Patent documents 1 and 2).

However, coenzyme-binding type GDHs generally exhibit a broad substrate specificity, and also react with maltose, galactose and so forth in addition to glucose. When they are applied as a glucose sensor for monitoring blood sugar levels of diabetic patients, and the diabetic patients have such severe symptoms that peritoneal dialysis must be performed, there is a risk that values higher than the true blood sugar levels may be obtained, because a large amount of maltose is contained in the dialysate. GDH derived from Burkholderia cepacia also exhibits reactivity to maltose and galactose in addition to glucose.

A technique of changing substrate specificity of GDH by introducing an amino acid substitution mutation is known. As such mutant GDHs, for example, there are known PQQGDHs derived from E. coli (Patent documents 3 and 4), Acinetobacter calcoaceticus (Gluconobacter calcoaceticus) (Patent document 5), and Acinetobacter baumannii (Patent documents 6 to 8) requiring pyroloquinoline quinone as a coenzyme.

[Patent document 1] U.S. Patent Application No. 2004/0023330 [Patent document 2] International Patent Publication [Patent document 3] Japanese Patent Laid-open (Kokai) No. [Patent document 4] Japanese Patent Laid-open No. 2001 [Patent document 5] Japanese Patent Laid-open No. 2004 [Patent document 6] Japanese Patent Laid-open No. 2004 [Patent document 7] Japanese Patent Laid-open No. 2004 [Patent document 8] Japanese Patent Laid-open No. 2004

DISCLOSURE OF THE INVENTION

An object of the present invention is to provide an FAD-binding type GDH showing an improved substrate specificity to glucose.

The inventors of the present invention conducted various researches in order to achieve the foregoing object. As a result, they found that by modifying the amino acid sequence of the FAD-binding type GDH derived from Burkholderia cepacia at a specific site, the reactivity thereof to sugars other than glucose could be decreased while maintaining the reactivity to glucose, and thus accomplished the present invention.

That is, the present invention provides the followings.

(1) A mutant glucose dehydrogenase exhibiting improved substrate specificity to glucose, which is a protein having the amino acid sequence of SEQ ID NO: 13 or an amino acid sequence of SEQ ID NO: 13 including substitution, deletion, insertion or addition of one or more amino acid residues at position other than the positions listed below and having a glucose dehydrogenase activity, and has any of the amino acid substitution mutations listed below (numerals represent a position in the amino acid sequence, the amino acid residues represent an amino acid residue after substitution at the position, and “+” means that two amino acid substitutions are simultaneously included):

(A) 472Arg, 472Asn, 472Asp, 472Cys, 472Glu, 472Gly, 472H is, 472Ile, 472Leu, 472Met, 472Phe, 472Pro, 472Ser, 472Trp, 472Tyr, 472Val, (B) 475Asp, 475Cys, 475Glu, 475Gly, 475H is, 475Met, 475Phe, 475Ser, 475Tyr, 475Val, (C) 472Arg+475(Asp, Glu, Gly, H is, Phe, Ser, Tyr), 472Asn+475(Asp, Gly, H is, Phe, Ser, Tyr), 472Asp+475(H is, Phe, Ser, Val), 472Cys+475(Asp, Gly, H is, Phe, Ser), 472Glu+475(Asp, Glu, Gly, H is, Phe, Ser, Tyr), 472Gly+475(Asp, Cys, Gly, Met, Phe, Ser, Tyr), 472His+475(Cys, Glu, H is, Met, Phe, Ser, Tyr), 472Ile+475(Asp, Cys, Glu, Gly, H is, Met, Phe, Ser, Tyr), 472Leu+475(Asp, Gly, H is, Phe, Ser, Tyr), 472Met+475(Asp, Gly, H is, Phe, Ser), 472Phe+475(Asp, Glu, Gly, H is, Met, Phe, Ser, Tyr), 472Pro+475His 472Ser+475(Asp, Glu, Gly, H is, Phe, Ser), 472Trp+475(H is, Phe, Ser), 472Tyr+475(Asp, His, Phe, Ser), 472Val+475(Asp, Glu, Gly, His, Phe, Ser).

(2) The aforementioned mutant glucose dehydrogenase, which has the amino acid sequence of SEQ ID NO: 13 provided that it includes any of the amino acid substitution mutations listed in the aforementioned (A) to (C). (3) The aforementioned mutant glucose dehydrogenase, which has an amino acid substitution mutation selected from the following mutations:

(D) 472Arg, 472Asn, 472Asp, 472Glu, 472Gly, 472Phe, 472Pro, (E) 475Asp, 475Cys, 475Glu, 475Gly, 475Met, 475Phe (F) 472Arg+475(Asp, Gly, His, Phe), 472Asn+475(Gly, His, Phe, Tyr), 472Asp+475(H is, Ser), 472Cys+475(Gly, His, Phe), 472Glu+475(Glu, His, Phe, Tyr), 472Gly+475(Asp, Phe, Tyr), 472His+475(H is, Ser), 472Ile+475(Asp, Glu, Gly, His, Ser), 472Leu+475(Gly, His, Phe, Tyr), 472Met+475(Asp, Gly, His, Phe), 472Phe+475(Asp, Glu, Gly, His, Phe, Ser, Tyr), 472Ser+475(Glu, Gly, His, Phe), 472Trp+475(H is, Phe), 472Tyr+475His, 472Val+475(Asp, Glu, Gly, His, Phe).

(4) A glucose dehydrogenase, which is a protein having the amino acid sequence of SEQ ID NO: 13 or an amino acid sequence of SEQ ID NO: 13 including substitution, deletion, insertion or addition of one or more amino acid residues at position other than the positions listed below and having a glucose dehydrogenase activity, and wherein: (i) at least either the arginine residue at position 472 or the asparagine residue at position 475 in the amino acid sequence of SEQ ID NO: 13 is replaced with another amino acid residue, and (ii) a ratio of specific activity for glucose and specific activity for maltose ((reactivity to maltose/reactivity to glucose)×100) of the glucose dehydrogenase introduced with the aforementioned mutation is reduced by 10% or more compared with that of a glucose dehydrogenase not introduced with the mutation. (5) A mutant glucose dehydrogenase complex comprising at least the aforementioned mutant glucose dehydrogenase and an electron transfer subunit. (6) A DNA coding for the aforementioned mutant glucose dehydrogenase. (7) A microorganism having the aforementioned DNA and producing the aforementioned mutant glucose dehydrogenase or the mutant glucose dehydrogenase complex. (8) A glucose assay kit comprising the aforementioned mutant glucose dehydrogenase, the mutant glucose dehydrogenase complex, or the microorganism. (9) A glucose sensor comprising the aforementioned mutant glucose dehydrogenase, the mutant glucose dehydrogenase complex, or the microorganism. In the present specification, although the term “mutant GDH” refers to a mutant α-subunit in the context of contrast with a mutant GDH complex, a mutant α-subunit and a mutant GDH complex may also be collectively referred to as “mutant GDH”.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows dehydrogenase activities of DH5α/pTrc99A/γ+α for glucose and maltose as substrates. The rhombuses represent the activity for glucose, and the squares represents the activity for maltose (the same shall apply in FIGS. 2 to 5).

FIG. 2 shows dehydrogenase activities of DH5α/pTrcγαAsn475Asp for glucose and maltose as substrates.

FIG. 3 shows dehydrogenase activities of DH5α/pTrc99Aγαβ for glucose and maltose as substrates.

FIG. 4 shows dehydrogenase activities of DH5α/pTrcγαβAsn475Asp for glucose and maltose as substrates.

FIG. 5 shows dehydrogenase activities of DH5α/pTrcγαβAsn475Glu for glucose and maltose as substrates.

FIG. 6 shows sequences of PCR primers used for codon substitutions at positions 472 and 475 in the GDH α-subunit.

FIG. 7 shows SV plots of mutant GDHs.

FIG. 8 shows SV plots of mutant GDHs.

FIG. 9 shows a structure of a glucose sensor.

FIG. 10 shows reagent parts of a glucose sensor.

FIG. 11 shows reactivity to glucose of a glucose sensor using a wild type GDH.

FIG. 12 shows reactivity to glucose of a glucose sensor using 472Glu475Tyr type GDH.

FIG. 13 shows reactivity to glucose of a glucose sensor using 472Asp475His type GDH.

FIG. 14 shows reactivity to maltose of a glucose sensor using a wild type GDH in the presence of glucose.

FIG. 15 shows reactivity to maltose of a glucose sensor using 472Glu475Tyr type GDH in the presence of glucose.

FIG. 16 shows reactivity to maltose of a glucose sensor using 472Asp475His type GDH in the presence of glucose.

FIG. 17 shows apparent blood sugar levels measured by using glucose sensors using a wild type GDH and a mutant GDH.

BEST MODE FOR CARRYING OUT THE INVENTION

Hereafter, the present invention will be explained in detail.

The mutant GDH of the present invention is produced by introducing a specific mutation into a wild type GDH. Examples of the wild type GDH include GDHs produced by Burkholderia cepacia. Examples of the GDHs produced by Burkholderia cepacia include GDHs produced by the Burkholderia cepacia KS1, JCM2800 and JCM2801 strains. The KS1 strain was deposited at the independent administrative corporation, National Institute of Advanced Industrial Science and Technology, International Patent Organism Depositary (Tsukuba Central 6, 1-1, Higashi 1-Chome, Tsukuba-shi, Ibaraki-ken, 305-8566, Japan) on Sep. 25, 2000 and given an accession number FERM BP-7306. The JCM2800 and JCM2801 strains are stored at the independent administrative corporation, RIKEN, Bioresource Center, Japan Collection of Microorganisms (JCM).

The nucleotide sequence of a chromosomal DNA fragment containing the GDH α-subunit gene and a part of the β-subunit gene of the KS1 strain is shown in SEQ ID NO: 11 (U.S. Patent Application No. 2004/0023330). Three open reading frames (ORF) exist in this nucleotide sequence, the second and third ORFs from the 5′ end side code for the α-subunit (SEQ ID NO: 13) and the β-subunit (SEQ ID NO: 14), respectively. Further, it is inferred that the first ORF codes for the γ-subunit (SEQ ID NO: 12). Further, the nucleotide sequence of a fragment containing the full-length β-subunit gene is shown in SEQ ID NO: 15. Further, the amino acid sequence of the β-subunit is shown in SEQ ID NO: 16. It is inferred that the amino acid numbers 1 to 22 in SEQ ID NO: 16 correspond to a signal peptide. Although the first amino acid residues are Val in SEQ ID NOS: 15 and 16, they are very likely to be Met and may be eliminated after translation.

The mutant GDH of the present invention may consist of the α-subunit alone, a complex comprising the α-subunit and the β-subunit, or a complex comprising the α-subunit, β-subunit and γ-subunit. The mutant GDH of the present invention is obtained by introducing a specific mutation into the α-subunit in any case, and may have a conservative mutation in addition to the above specific mutation. Further, the other subunits may be of a wild type or have a conservative mutation. The term “conservative mutation” means a mutation that does not substantially affect the GDH activity.

The mutant α-subunit of the present invention preferably has the amino acid sequence of SEQ ID NO: 13 except that it includes the specific mutation described later. Further, the mutant α-subunit may have the aforementioned conservative mutation so long as it has the GDH activity. That is, it may be a protein having an amino acid sequence of SEQ ID NO: 13 including substitution, deletion, insertion or addition of one or more amino acid residues in addition to the aforementioned specific mutation. SEQ ID NO: 13 shows an amino acid sequence that can be encoded by the nucleotide sequence of SEQ ID NO: 11. However, the methionine residue at the N-terminus may be eliminated after translation. The aforementioned term “one or several” preferably means a number of 1 to 10, more preferably 1 to 5, particularly preferably 1 to 3.

Further, the β-subunit typically has the amino acid sequence of SEQ ID NO: 16. However, so long as it functions as the β-subunit of GDH, it may be a protein having an amino acid sequence of the amino acid numbers 23 to 425 of SEQ ID NO: 16 including substitution, deletion, insertion or addition of one or more amino acid residues. The aforementioned term “one or several” preferably means a number of 1 to 20, more preferably 1 to 10, particularly preferably 1 to 5. The expression “functions as the GDH β-subunit” means to function as cytochrome C without degrading the enzymatic activity of GDH.

Specific examples of the wild type α-subunit gene include a DNA containing the nucleotide sequence corresponding to the nucleotide numbers 764 to 2380 of SEQ ID NO: 11. Further, the α-subunit gene may be a DNA having the nucleotide sequence corresponding to the nucleotide numbers 764 to 2380 in the nucleotide sequence of SEQ ID NO: 11 or a DNA which is hybridizable with a probe prepared from that sequence under a stringent condition and codes for a protein having the GDH activity.

Further, specific examples of the β-subunit gene include a DNA having the nucleotide sequence corresponding to the nucleotide numbers 187 to 1398 of SEQ ID NO: 9. Further, the β-subunit gene may be a DNA which has the nucleotide sequence corresponding to the nucleotide numbers 187 to 1398 of SEQ ID NO: 9, or a DNA which is hybridizable with a probe prepared from that sequence under a stringent condition and codes for a protein that can function as the β-subunit.

Examples of the aforementioned stringent condition include, for example, a condition under which DNAs having a homology of 70% or more, preferably 80% or more, more preferably 90% or more, particularly preferably 95% or more, hybridize with each other, and it is specifically exemplified by the condition of 1×SSC, 0.1% SDS at 60° C.

The α-subunit gene and the β-subunit gene can be obtained by, for example, PCR using chromosomal DNA of the Burkhorderia cepacia KS1 strain as a template. Primers for PCR can be prepared by chemical synthesis on the basis of the aforementioned nucleotide sequences. Further, they can also be obtained from chromosomal DNA of the Burkhorderia cepacia KS1 strain by hybridization using an oligonucleotide prepared on the basis of the aforementioned sequences as a probe. Further, variants thereof can also be similarly obtained from other strains of Burkhorderia cepacia. Examples of the other bacterial strains include the aforementioned JCM2800 and JCM2801 strains. The α-subunits of GDHs produced by these strains have homologies of 95.4 and 93.7%, respectively, to the α-subunit of the KS1 strain.

Further, even GDHs produced by other microorganisms can be used for the production of mutant GDH of the present invention so long as they have a structure and enzymological characteristics similar to those of GDH produced by Burkhorderia cepacia.

In the mutant GDH of the present invention, substrate specificity to glucose is improved by introducing a specific mutation into the aforementioned wild type GDH. The expression “substrate specificity to glucose is improved” means that reactivity to other sugars such as monosaccharides, disaccharide and oligosaccharides, for example, maltose, galactose, xylose and so forth, is decreased while the reactivity to glucose is substantially maintained, or reactivity to glucose is improved compared with reactivities to other sugars. For example, even if reactivity to glucose is decreased, but if reactivities to other sugars are decreased to a greater extent, substrate specificity to glucose is improved. Further, even if reactivities to other sugars are increased, but if substrate specificity to glucose is increased to a greater extent, substrate specificity to glucose is improved. Specifically, for example, if the ratio of specific activity for glucose and specific activity for another sugar, for example, maltose ((reactivity to another sugar/reactivity to glucose)×100) is decreased by 10% or more, preferably 20% or more, more preferably 50% or more, substrate specificity to L glucose is improved.

The aforementioned specific mutation means any one of amino acid substitution at position 472, amino acid substitution at position 475 and amino acid substitution at both positions 472 and 475 in the amino acid sequence of the SEQ ID NO: 13. More specific examples of the mutation include amino acid substitutions described below. The numerals shown below represent a position in the amino acid sequence, the amino acid residues represent an amino acid residue after substitution at the aforementioned position, and “+” means that two amino acid substitutions are simultaneously included. Among the following amino acid substitutions, amino acid substitutions at position 472 are listed in (A), amino acid substitutions at position 475 are listed in (B), and amino acid substitutions at both positions 472 and 475 are listed in (C). For example, “472Asn+475(Asp, Gly, His, Phe, Ser, Tyr)” means mutations for substitution of Asn for the amino acid residue at position 472 (Ala in the wild type), and substitution of Asp, Gly, His, Phe, Ser or Tyr for the amino acid residue at position 475 (Asn in the wild type).

(A) 472Arg, 472Asn, 472Asp, 472Cys, 472Glu, 472Gly, 472His, 472Ile, 472Leu, 472Met, 472Phe, 472Pro, 472Ser, 472Trp, 472Tyr, 472Val, (B) 475Asp, 475Cys, 475Glu, 475Gly, 475His, 475Met, 475Phe, 475Ser, 475Tyr, 475Val, (C) 472Arg+475(Asp, Glu, Gly, His, Phe, Ser, Tyr), 472Asn+475(Asp, Gly, His, Phe, Ser, Tyr), 472Asp+475(H is, Phe, Ser, Val), 472Cys+475(Asp, Gly, His, Phe, Ser), 472Glu+475(Asp, Glu, Gly, His, Phe, Ser, Tyr), 472Gly+475(Asp, Cys, Gly, Met, Phe, Ser, Tyr), 472His+475(Cys, Glu, His, Met, Phe, Ser, Tyr), 472Ile+475(Asp, Cys, Glu, Gly, His, Met, Phe, Ser, Tyr), 472Leu+475(Asp, Gly, His, Phe, Ser, Tyr), 472Met+475(Asp, Gly, His, Phe, Ser), 472Phe+475(Asp, Glu, Gly, His, Met, Phe, Ser, Tyr), 472Pro+475His 472Ser+475(Asp, Glu, Gly, His, Phe, Ser), 472Trp+475(H is, Phe, Ser), 472Tyr+475(Asp, His, Phe, Ser), 472Val+475(Asp, Glu, Gly, His, Phe, Ser).

Among the aforementioned amino acid substitutions, preferred are listed below.

(D) 472Arg, 472Asn, 472Asp, 472Glu, 472Gly, 472Phe, 472Pro, (E) 475Asp, 475Cys, 475Glu, 475Gly, 475Met, 475Phe (F) 472Arg+475(Asp, Gly, His, Phe), 472Asn+475(Gly, His, Phe, Tyr), 472Asp+475(H is, Ser), 472Cys+475(Gly, His, Phe), 472Glu+475(Glu, His, Phe, Tyr), 472Gly+475(Asp, Phe, Tyr), 472His+475(H is, Ser), 472Ile+475(Asp, Glu, Gly, His, Ser), 472Leu+475(Gly, His, Phe, Tyr), 472Met+475(Asp, Gly, His, Phe), 472Phe+475(Asp, Glu, Gly, His, Phe, Ser, Tyr), 472Ser+475(Glu, Gly, His, Phe), 472Trp+475(H is, Phe), 472Tyr+475His, 472Val+475(Asp, Glu, Gly, His, Phe).

The positions of the aforementioned amino acid substitution mutations are those in SEQ ID NO: 13, that is, the amino acid sequence of the wild type GDH α-subunit of the Burkholderia cepacia KS1 strain, and in a GDH α-subunit homologue or variant having an amino acid sequence containing substitution, deletion, insertion or addition of one or more amino acid residues in the amino acid sequence of SEQ ID NO: 13 in addition to the aforementioned specific mutations, the positions are those corresponding to the positions of aforementioned amino acid substitutions determined by alignment with the amino acid sequence of SEQ ID NO: 13. For example, in a conservative GDH α-subunit variant having deletion of one amino acid residue in the region of 1st to 471st positions, the 472nd and 475th positions represent the 471st and 474th positions in the variant.

The inventors of the present invention investigated the region of glucose dehydrogenase involved in binding to FAD and neighboring regions as positions for introduction of the mutation for improving the substrate specificity. As the region involved in binding to FAD, the FAD neighboring region (FAD-covering lid) or FAD-binding domain, specifically, regions corresponding to the amino acid sequences of SEQ ID NOS: 1 to 4, were contemplated.

The term “regions corresponding to amino acid sequences” means, in the GDH α-subunit of the Burkhorderia cepacia KS1 strain having the amino acid sequence of SEQ ID NO: 13, regions having the amino acid sequence of SEQ ID NO: 1, 2 or 4, that is, regions of the amino acid numbers 88 to 92, 57 to 61, and 470 to 504 in SEQ ID NO: 13. Further, in the GDH α-subunit having an amino acid sequence homologous to the amino acid sequence of SEQ ID NO: 13, the regions are those corresponding to the regions of the amino acid numbers 88 to 92, 57 to 61 or 470 to 504 in the GDH α-subunit of the aforementioned Burkhorderia cepacia KS1 strain determined by alignment with the amino acid sequence of SEQ ID NO: 13.

The inventors of the present invention compared the amino acid sequences of the GMC oxidoreductase family enzymes using FAD as a coenzyme, sorbitol dehydrogenase of Gluconobacter oxydans (GenBank accession AB039821), 2-ketoglutarate dehydrogenase of Erwinia herbicola (GenBank accession AF068066), cellobiose dehydrogenase (CDH) of Phanerochaete chrysosporium (J. Mol. Biol., 315(3), 421-34 (2002)), cholesterol oxidase (COD) of Streptomyces species (J. Struct. Biol. 116(2), 317-9 (1996)), and glucose oxidase of Penicillium amagasakiens (Eur. J. Biochem. 252, 90-99 (1998)), and found a region in which the FAD-binding domain and FAD-covering lid were conserved and a region in which proline was conserved, which is an amino acid residue involved in folding of proteins. Then, they examined the possibility of improving substrate specificity by modifying sequences in the vicinity of the borders between these regions and other regions. As a result, they confirmed that the substrate specificity could be improved by mutations of the aforementioned amino acid residues.

A GDH α-subunit having a desired mutation can be obtained by introducing a nucleotide mutation corresponding to a desired amino acid mutation into a DNA coding for the GDH α-subunit (α-subunit gene) by site-directed mutagenesis and expressing the obtained mutant DNA by using a suitable expression system. Further, a mutant GDH complex can be obtained by expressing a DNA coding for the mutant GDH α-subunit together with a DNA coding for the β-subunit (β-subunit gene) or the β-subunit gene and a DNA coding for the γ-subunit (γ-subunit gene). For the introduction of a mutation into a DNA coding for the GDH α-subunit, a polycistronic DNA fragment coding for the GDH α-subunit, γ-subunit and β-subunit in this order may also be used.

Substrate specificities to sugars of the GDH α-subunit or the GDH complex introduced with the mutation can be determined by examining reactivities to various sugars by the methods described in the examples and comparing them with reactivities of a wild type GDH α-subunit or a wild type GDH complex.

A polycistronic DNA fragment coding for the γ-subunit, α-subunit and β-subunit in this order can be obtained by, for example, PCR using chromosomal DNA of the Burkhorderia cepacia KS1 strain as a template and oligonucleotides having the nucleotide sequences of SEQ ID NOS: 12 and 13 as primers (see the examples described later).

Examples of vectors used for obtaining the genes of GDH subunits, introduction of mutation, expression of the genes and so forth include vectors that function in Escherichia bacteria, and specific examples thereof include pTrc99A, pBR322, pUC18, pUC118, pUC19, pUC119, pACYC184, pBBR122 and so forth. Examples of the promoters used for expression of genes include lac, trp, tac, trc, P_(L), tet, PhoA and so forth. Further, insertion of these genes into a vector and ligation of a promoter can be performed in one step by inserting the α-subunit gene or other subunit genes at a suitable site in an expression vector containing the promoter. Examples of such an expression vector include pTrc99A, pBluescript, pKK223-3 and so forth.

Further, the α-subunit gene or other subunit genes may be incorporated into chromosomal DNA of a host microorganism in an expressible form.

Examples of the method for transforming a microorganism with a recombinant vector include, for example, the competent cell method using a calcium treatment, protoplast method, electroporation and so forth.

Examples of the host microorganism include Bacillus bacteria such as Bacillus subtilits, yeast such as Saccharomyces cerevisiae and filamentous fungi such as Aspergillus niger. However, the host microorganism is not limited to these examples, and host microorganisms suitable for producing foreign proteins can be used.

The mutant α-subunit, the mutant GDH complex, and the microorganism expressing them of the present invention can be used as an enzyme electrode of a glucose sensor or a component of a glucose assay kit. A glucose sensor and glucose assay kit using the wild type GDH of Burkhorderia cepacia are described in U.S. Patent No. 2004/0023330A1. The mutant GDH of the present invention can also be used in a similar manner.

EXAMPLES

The present invention will be explained more specifically with reference to the following examples. However, the scope of the present invention is not limited to these examples.

Example 1 Plasmids expressing GDH of Burkhorderia cepacia

As plasmids expressing GDH of Burkhorderia cepacia, a plasmid expressing the GDH α-subunit and γ-subunit and a plasmid expressing the α-subunit, β-subunit and γ-subunit were prepared.

<1>Plasmid Expressing GDH α-Subunit and γ-Subunit

As a plasmid expressing the α-subunit and γ-subunit, plasmid pTrc99A/γ+α described in WO02/036779 was used. This plasmid is a plasmid obtained by inserting a DNA fragment sequentially containing the GDH γ-subunit structural gene and the α-subunit structural gene isolated from chromosomal DNA of the Burkhorderia cepacia KS1 strain (FERM BP-7306) into the vector pTrc99A (Pharmacia) at the NcoI/HindIII site as a cloning site thereof. The GDHγα gene in this plasmid is regulated by the trc promoter. pTrc99A/γ+α has an ampicillin resistance gene.

<2>Plasmid Expressing GDH α-Subunit, β-Subunit and γ-Subunit

A plasmid expressing the GDH α-subunit, β-subunit and γ-subunit was prepared as follows.

(1) Preparation of Chromosomal DNA from Burkhorderia cepacia KS1 Strain

A chromosomal gene was prepared from the Burkhorderia cepacia KS1 strain in a conventional manner. That is, the TL liquid medium (10 g of polypeptone, 1 g of yeast extract, 5 g of NaCl, 2 g of KH₂PO₄, 5 g of glucose in 1 L, pH 7.2) was used, and cells of the strain was shaken overnight in the medium at 34° C. The grown cells were collected by centrifugation. The cells were suspended in a solution containing 10 mM NaCl, 20 mM Tris-HCl (pH 8.0), 1 mM EDTA, 0.5% SDS and 100 μg/ml of proteinase K and treated at 50° C. for 6 hours. To the mixture was added an equal volume of phenol-chloroform, and the mixture was stirred at room temperature for 10 minutes. Then, the supernatant was collected by centrifugation. To the supernatant was added sodium acetate at a final concentration of 0.3 M, and 2-fold volume of ethanol was overlaid to precipitate chromosomal DNA in the intermediate layer. The DNA was collected with a glass rod, washed with 70% ethanol, and then dissolved in a suitable volume of TE buffer to obtain a chromosomal DNA solution.

(2) Preparation of DNA Fragment Coding for GDH γ-subunit, α-subunit and β-subunit

A DNA fragment coding for the GDH γ-subunit, α-subunit and β-subunit was amplified by PCR using the aforementioned chromosomal DNA as a template and oligonucleotides having the following sequences as primers.

[Forward primer] (SEQ ID NO: 5) 5′-CATGCCATGGCACACAACGACAACAC-3′ [Reverse primer] (SEQ ID NO: 6) 5′-GTCGACGATCTTCTTCCAGCCGAACATCAC-3′

The C-terminus side of the amplified fragment was blunt-ended, the N-terminus side was digested with NcoI, and the fragment was ligated to similarly treated pTrc99A (Pharmacia). E. coli DH5α was transformed with the obtained recombinant vector, and colonies grown on the LB agar medium containing 50 μg/mL of ampicillin were collected. The obtained transformants were cultured in the liquid LB medium, plasmids were extracted, and DNA fragments inserted in the plasmids were analyzed. As a result, an inserted fragment of about 3.8 kb was confirmed. This plasmid was designated as pTrc99Aγαβ. The structural genes of GDH in this plasmid are regulated by the trc promoter. pTrc99Aγαβ has an ampicillin resistance gene and a kanamycin resistance gene.

Example 2 Introduction of Mutation into GDH α-Subunit Gene

By using a commercially available site-directed mutatgenesis kit (QuikChangeII Site-Directed Mutagenesis Kit, Stratagene), the codon of aspartic acid (GAT) or glutamic acid (GAA) was substituted for the codon of the 475th asparagine (AAT) in the GDH α-subunit gene contained in the plasmids pTrc99A/γ+α and pTrc99Aγαβ described in Example 1. As primers, the following oligonucleotides were used. Hereinafter, substitution of an aspartic acid residue for the 475th asparagine residue is referred to as “Asn475Asp”, and substitution of a glutamic acid residue for the 475th asparagine residue is referred to as “Asn475Glu”.

Primers for Asn475Asp substitution [Forward primer] (SEQ ID NO: 7) 5′-CGCGCCGAACGATCACATCACGGGC-3′ [Reverse primer] (SEQ ID NO: 8) 5′-GCCCGTGATGTGATCGTTCGGCGCG-3′ Primers for Asn475Glu substitution [Forward primer] (SEQ ID NO: 9) 5′-GAATTCGCGCCGAACGAACACATCAGGGGCTCG-3′ [Reverse primer] (SEQ ID NO: 10) 5′-CGAGCCCGTGATGTGTTCGTTCGGCGCGAATTC-3′

PCR was performed by using the following reaction composition. After a reaction at 95° C. for 30 seconds, a cycle of reactions at 95° C. for 30 seconds, 55° C. for 1 minute and 68° C. for 8 minutes was repeated 15 times. Then, after a reaction at 68° C. for 30 minutes, the reaction mixture was maintained at 4° C.

[Reaction mixture composition] Template DNA (5 ng/μl) 2 μl (pTrc99A/γ + α and pTrc99Aγαβ) 10× Reaction buffer 5 μl Forward primer (100 ng/μl) 1.25 μl Reverse primer (100 ng/μl) 1.25 μl dNTP 1 μl Distilled water 38.5 μl DNA polymerase 1 μl Total 50 μl

After PCR, 0.5 μl of DNA polymerase I was added to the reaction mixture, and the mixture was incubated at 37° C. for 1 hour to decompose the template plasmid.

Competent cells of Escherichia coli DH5α (supE44, ΔlacU169 (φ+80lacZΔM15), hsdR17, recA1, endA1, gyrA96, thi-1, relA1) were transformed with the obtained reaction mixture. Plasmid DNA was prepared from several colonies grown on the LB agar medium (1% bacto tryptone, 0.5% yeast extract, 1% sodium chloride, 1.5% agar) containing ampicillin (50 μg/ml) and kanamycin (30 μg/ml), and sequence analysis was performed to confirm that the objective mutations had been introduced into the GDH α-subunit gene. pTrc99A/γ+α and pTrc99Aγαβ introduced with the Asn475Asp mutation were designated as pTrcγαAsn475Asp and pTrcγαβAsn475Asp, respectively. Further, pTrc99A/γ+α and pTrc99Aγαβ introduced with the Asn475Glu mutation were designated as pTrcγαAsn475Glu and pTrcγαβAsn475Glu, respectively.

Example 3 Analysis of Substrate Specificity of Mutant GDHs

Mutant GDHs were produced by using the mutant GDH expressing plasmids obtained in Example 2, and substrate specificities thereof were examined.

(1) Culture

The Escherichia coli DH5a strain introduced with pTrcγαAsn475Glu and pTrcγαβAsn475Glu were each cultured overnight at 37° C. in 2 ml of the LB medium (containing 50 μg/ml of ampicillin and 30 μg/ml of kanamycin) in an L-shaped tube with shaking. These culture broths were inoculated in 150 ml of the LB medium (containing 50 μg/ml of ampicillin and 30 μg/ml of kanamycin) contained in a 500-ml Sakaguchi flask, and the cells were cultured at 37° C. with shaking. After 3 hours from the start of culture, isopropyl-β-D-thiogalactopyranoside (IPTG) was added at a final concentration of 0.1 mM, and the cells were further cultured for 2 hours.

(2) Preparation of Enzyme Samples

The cells were collected from each culture broth obtained as described above, washed, then suspended in 10 mM potassium phosphate buffer (PPB, pH 7.0) containing 1 ml of 0.2% Triton X-100 per 0.3 mg of wet cells, and disrupted by ultrasonication. This suspension was centrifuged (10000 rpm, 10 min, 4° C.) to remove the residues, then the supernatant was ultracentrifuged (50,000 r.p.m., 60 min, 4° C.), and the obtained supernatant (water-soluble fraction) was used as a crude enzyme sample. Further, this sample was purified by usual hydrophobic chromatography (column: Octyl Sepharose, Amersham Biosciences) and ion exchange chromatography (Q-Sepharose, Amersham Biosciences) to obtain a purified enzyme sample. The objective enzyme fraction was determined by using GDH activity as an index.

(3) Measurement of GDH Activity

To 8 μl of the aforementioned purified enzyme sample was added 8 μl of a reagent for measuring activity (solution obtained by adding 10 mM PPB containing 0.2% (w/v) Triton X-100 to 12 μl of 600 mM methylphenazine methosulfate (PMS) and 120 μl of 6 mM 2,6-dichrolophenol-indophenol (DCIP) to make a total volume of 480 μl). This mixture was preincubated at each reaction temperature for one minute by using an aluminum block thermostatic chamber, then 8 μl of a substrate (glucose or maltose) at each concentration or distilled water was quickly added to the mixture, and the mixture was stirred. Absorbance at 600 nm as the DCIP-originated absorption wavelength was measured by using a spectrophotometer. The final concentrations of the reagents, DCIP and PMS, were 0.06 and 0.6 mM, respectively. The final concentrations of the substrate were 40, 20, 10 and 5 mM.

The results are shown in Table 1 and FIGS. 1 to 5.

TABLE 1 Substrate concentration Activity (U/ml) mM Glucose Maltose pTrc99A/γ + α 40 1.65 1.01 20 1.70 1.03 10 1.71 1.07 5 1.57 0.72 pTrcγαAsn475Asp 40 19.46 1.30 20 7.75 0.67 10 4.15 0.21 5 2.53 0.00 pTrc99Aγαβ 40 5.49 1.82 20 5.38 1.78 10 5.03 1.57 5 4.20 1.24 pTrcγαβAsn475Asp 40 11.57 1.35 20 6.53 0.93 10 3.21 0.39 5 2.50 0.13 pTrcγαβAsn475Glu 40 8.62 2.10 20 7.13 1.26 10 6.12 0.84 5 4.95 0.43

As clearly seen form these results, it is evident that all the mutant GDHs have reduced reactivity to maltose while maintaining reactivity to glucose, that is, their specificity to glucose is improved.

Example 4 Introduction of Mutation into GDH α-Subunit Gene

Mutations were introduced into the GDH α-subunit gene contained in pTrc99Aγαβ obtained in Example 1 at the 475th position and neighboring positions, and substrate specificity of the mutant enzymes was evaluated. Mutations were introduced in the same manner as in Example 2. Primers for introducing mutations were prepared as follows. In the basic primers (wild type) shown in FIG. 6 (forward primer: SEQ ID NO: 17, reverse primer: SEQ ID NO: 18), codons were changed at predetermined positions (472nd and 475th) as shown in the codon change table mentioned in FIG. 6 to prepare primers for introducing various mutations.

Example 5 Analysis of Substrate Specificity of Mutant GDHs

Mutant GDHs were produced in the same manner as in Example 3 by using the mutant GDH expressing plasmids obtained in Example 4, and substrate specificities thereof were examined. The enzymatic activity was examined by using crude enzyme samples. The specific activity for glucose, specific activity for maltose and reaction ratio (specific activity for maltose/specific activity for glucose, unit is U/ml.) of each mutant GDH are shown in Tables 2 to 7. When the specific activity for glucose was 0.5 U/ml or lower, it was judged as no activity, and such a result was indicated with “−” in the tables.

As a result, for the 475th position, it was confirmed that substitutions other than the substitution of aspartic acid (GAT) or glutamic acid (GAA) for asparagine performed in Example 2 also had an effect of improving the substrate characteristics. Further, it was found that substitution of another amino acid for asparagine (AAC) at the 472nd position in the vicinity of the 475th position could also improve the substrate characteristics. Further, it was also found that a combination of the amino acid substitutions at the 472nd and 475th positions could synergistically improve the substrate characteristics.

TABLE 2 substrate conc.: 10 mM specific activity to glucose (U/ml broth) 475 472 Ala Arg Asn Asp Cys Glu Gln Gly His Ile Ala — — 7 6.5 24 7 — 4.75 0.85 — Arg — — 6 2.35 — 1.5 — 2.3 2.4 — Asn — — 6.2 0.75 — — — 2.3 4.7 — Asp — — 1.35 — — — — — 1.75 — Cys — — 6.45 0.75 — — — 4 4.3 — Glu — — 6.1 2.15 — 1.2 — 3.45 4.65 — Gln — — — — — — — — — — Gly — — 6.35 0.6 1 — — 6.85 — — His — — 4.45 — 0.85 2.75 — — 4.4 — Ile — — 7.25 2.4 0.75 2.2 — 2.1 4.4 — Leu — — 6.35 0.75 — — — 1.9 5.65 — Lys — — — — — — — — — — Met — — 5.9 1.85 — — — 3.3 5.8 — Phe — — 6.79 0.65 — 0.55 — 1.75 6.25 — Pro — — 1.2 — — — — — 2.3 — Ser — — 6.1 1.1 — 2.45 — 4.25 4 — Thr — — — — — — — — — — Trp — — 4.55 — — — — — 6.3 — Tyr — — 4.35 0.5 — — — — 5.75 — Val — — 5.75 2.2 — 0.85 — 2.5 5.9 —

TABLE 3 substrate conc.: 10 mM specific activity to maltose (U/ml broth) 475 472 Ala Arg Asn Asp Cys Glu Gln Gly His Ile Ala — — 3.5 1 0.55 1.5 — 1.35 0.8 — Arg — — 0.85 0.25 — 0.35 — 0.25 0.35 — Asn — — 0.75 0.21 — — — 0.28 0.44 — Asp — — 0.1 — — — — — 0.25 — Cys — — 1.2 0.18 — — — 0.2 0.41 — Glu — — 0.7 0.85 — 0.15 — 0.35 0.41 — Gln — — — — — — — — — — Gly — — 0.8 0.08 0.3 — — 1.55 — — His — — 1.05 — 0.2 0.5 — — 0.5 — Ile — — 0.85 0.2 0.1 0.2 — 0.33 0.45 — Leu — — 1.2 0.2 — — — 0.3 0.45 — Lys — — — — — — — — — — Met — — 1.1 0.25 — — — 0.34 0.45 — Phe — — 0.81 0.09 — 0.09 — 0.25 0.45 — Pro — — 0.15 — — — — — 0.6 — Ser — — 1.25 0.24 — 0.25 — 0.5 0.4 — Thr — — — — — — — — — — Trp — — 1.1 — — — — — 0.6 — Tyr — — 1.05 0.14 — — — — 0.35 — Val — — 1.1 0.2 — 0.1 — 0.22 0.49 —

TABLE 4 substrate conc.: 10 mM maltose/glucose (reaction ratio) 475 472 Ala Arg Asn Asp Cys Glu Gln Gly His Ile Ala — — 50% 15% 23% 21% — 28% 94% — Arg — — 14% 10% — 23% — 11% 14% — Asn — — 12% 27% — — — 12%  9% — Asp — —  7% — — — — — 14% — Cys — — 19% 24% — — —  5% 10% — Glu — — 11% 40% — 13% — 10%  9% — Gln — — — — — — — — — — Gly — — 13% 13% 30% — — 23% — — His — — 24% — 24% 18% — — 11% — Ile — — 12%  8% 13%  9% — 16% 10% — Leu — — 19% 27% — — — 16%  8% — Lys — — — — — — — — — — Met — — 19% 14% — — — 10%  8% — Phe — — 12% 13% — 15% — 14%  7% — Pro — — 13% — — — — — 26% — Ser — — 20% 22% — 10% — 12% 10% — Thr — — — — — — — — — — Trp — — 24% — — — — — 10% — Tyr — — 24% 27% — — — —  6% — Val — — 19%  9% — 12% —  9%  8% — Total: 60

TABLE 5 substrate conc.: 10 mM specific activity to glucose (U/ml broth) 475 472 Leu Lys Met Phe Pro Ser Thr Trp Tyr Val Ala — — 1.6 1.2 — 0.3 — — 1.05 1.15 Arg — — — 4.1 — 4.25 — — 2 — Asn — — — 2.5 — 5.25 — — 1.3 — Asp — — — 2.65 — 3 — — — 6.2 Cys — — — 2.85 — 4.5 — — — — Glu — — — 1.4 — 6 — — 1.9 — Gln — — — — — — — — — Gly — — 3.1 3.25 — 8 — — 0.5 — His — — 1.1 1.9 — 6.6 — — — — Ile — — 2.7 2.95 — 7 — — 3 — Leu — — — 1.6 — 5.5 — — 2 — Lys — — — — — — — — — Met — — — 3.25 — 4.6 — — — — Phe — — 1.7 0.75 — 10.5 — — 1.55 — Pro — — — — — — — — — Ser — — — 2.5 — 5.5 — — — — Thr — — — — — — — — — Trp — — — 3.5 — 2.15 — — — — Tyr — — — 0.85 — 3.85 — — — — Val — — — 3.5 — 7 — — 2.8 —

TABLE 6 substrate conc.: 10 mM specific activity to maltose (U/ml broth) 475 472 Leu Lys Met Phe Pro Ser Thr Trp Tyr Val Ala — — 0.5 0.35 — 0.25 — — 0.65 1.05 Arg — — 0.26 — 1.7 — — 0.33 Asn — — 0.45 — 1.1 — — 0.18 Asp — — 0.75 — 0.4 — — 3.3 Cys — — 0.2 — 0.95 — — Glu — — 0.15 — 1.15 — — 0.07 Gln — — — — — Gly — — 0.55 0.4 — 5 — — 0.05 His — — 0.22 0.35 — 0.75 — — Ile — — 0.95 0.6 — 0.5 — — 0.7 Leu — — 0.12 — 1.3 — — 0.25 Lys — — — — — Met — — 0.2 — 1.1 — — Phe — — 0.75 0.07 — 0.65 — — 0.2 Pro — — — — — Ser — — 0.2 — 1.3 — — Thr — — — — — Trp — — 0.2 — 0.55 — — Tyr — — 0.15 — 1.1 — — Val — — 0.2 — 1.2 — —

TABLE 7 substrate conc.: 10 mM maltose/glucose (reaction ratio) 475 472 Leu Lys Met Phe Pro Ser Thr Trp Tyr Val Ala — — 31% 29% — 83% — — 62% 91% Arg — — —  6% — 40% — — 16% — Asn — — — 18% — 21% — — 13% — Asp — — — 28% — 13% — — — 53% Cys — — —  7% — 21% — — — — Glu — — — 11% — 19% — —  3% — Gln — — — — — — — — — — Gly — — 18% 12% — 63% — — 10% — His — — 20% 18% — 11% — — — — Ile — — 35% 20% —  7% — — 23% — Leu — — —  8% — 24% — — 13% — Lys — — — — — — — — — — Met — — —  6% — 24% — — — — Phe — — 44%  9% —  6% — — 13% — Pro — — — — — — — — — — Ser — — —  8% — 24% — — — — Thr — — — — — — — — — — Trp — — —  6% — 26% — — — — Tyr — — — 18% — 29% — — — — Val — — —  6% — 17% — — — — Total: 60

Example 6 Evaluation of Purified Enzymes Based on SV Plot

SV plots were obtained for several mutant GDHs which showed improved substrate specificity in Example 5. Each mutant GDH was purified in the same manner as in Example 3. The results are shown in FIGS. 7 and 8 and Table 8.

As a result, it was confirmed that the reaction ratios (specific activity for maltose/specific activity for glucose) of the purified enzymes were also improved and became lower than that of the wild type at all the examined substrate concentrations. Further, since the results were substantially consistent with the measurement results using the crude enzyme solutions in Example 5, sufficient feasibility of screening for modified enzymes using crude enzymes could be confirmed. Further, modified enzymes to be used for a glucose sensor were selected from these candidates. For this purpose, since the blood maltose level elevates up to 200 mg/dl even at most, attentions were paid particularly to the reaction ratios at the substrate concentrations of 180 and 90 mg/dl. As a result, 472Asp475His was selected as a candidate of which reactivity to glucose was not so decreased compared with the wild type, and 472Glu475Tyr was selected as a candidate of which reactivity to glucose decreased but hardly reacted with maltose.

TABLE 8 Evaluation of characteristics of enzymes U/mg-p substrate conc. 1440 720 360 180 90 45 22.5 11.25 mg/dl reactivity to glucose wild-type 2198.8 2175.0 2035.8 1750.7 1264.6 803.7 461.7 244.0 472F 1123.3 1004.7 824.7 484.0 280.3 128.4 40.2 5.4 472D475F 811.5 678.6 512.5 328.9 215.3 107.3 33.7 4.1 475D 1324.4 1025.2 730.2 460.7 275.5 136.1 59.1 16.7 472D475H 2979.1 2522.1 1978.3 1322.9 795.0 430.8 207.1 82.9 472E475F 2153.8 1600.9 1079.9 667.3 366.0 165.6 46.6 7.0 472E475Y 734.4 466.8 219.5 88.2 17.4 2.4 0.8 0.2 475E 1296.4 768.2 426.0 209.6 reactivity to maltose wild-type 975.5 763.8 532.1 323.9 157.3 59.7 14.1 1.3 472F 215.4 133.6 58.9 10.3 2.3 0.6 0.3 0.3 472D475F 265.4 138.9 51.2 7.7 1.2 0.3 0.2 0.2 475D 290.1 197.4 116.2 48.8 13.0 1.4 0.4 0.2 472D475H 342.6 228.5 131.9 59.6 17.1 3.6 0.9 0.4 472E475F 544.1 304.8 137.2 39.7 5.5 1.4 0.4 0.2 472E475Y 23.3 4.2 1.3 0.4 0.3 0.1 0.2 0.0 475E 193.9 73.0 14.3 1.5 reaction ratio: maltose/glucose wild-type 44.4% 35.1% 26.1% 18.5% 12.4% 7.4% 3.1% 0.5% 472F 19.2% 13.3% 7.1% 2.1% 0.8% 0.5% 0.6% 4.7% 472D475F 32.7% 20.5% 10.0% 2.3% 0.6% 0.3% 0.5% 3.8% 475D 21.9% 19.3% 15.9% 10.6% 4.7% 1.1% 0.6% 1.0% 472D475H 11.5% 9.1% 6.7% 4.5% 2.1% 0.8% 0.4% 0.4% 472E475F 25.3% 19.0% 12.7% 5.9% 1.5% 0.8% 1.0% 2.5% 472E475Y 3.2% 0.9% 0.6% 0.5% 1.7% 3.5% 25.0% 0.0% 475E 15.0% 9.5% 3.4% 0.7%

Example 7 Preparation of Calorimetric Sensor for Measuring Blood Sugar Levels using Mutant GDHs

Colorimetric sensors for measuring blood sugar level were prepared by using 472Asp+475His type mutant GDH and 472Glu+475Tyr type mutant GDH.

A glucose sensor (1) having a basic structure shown in FIG. 9 was prepared. That is, the aforementioned glucose sensor had a configuration that a transparent cover (4) (material: PET) was laminated on a transparent base plate (2) via a spacer (3), and the capillary (5) was defined by the elements (2) to (4). The dimension of the capillary (5) was 1.3 mm×9 mm×50 μm (FIG. 9). The transparent base plate (2) and the transparent cover (4) were formed with PET having a thickness of 250 μm, and the spacer (3) was formed with a black double-sided tape.

The glucose sensor had a first reagent part (1), a second reagent part (2) and a third reagent part (3) shown in FIG. 10, and ingredients and coating amounts for each part are shown in Table 9. In the table, “Ru” represents a ruthenium hexaammine complex (Ru(NH₃)₆Cl₃), CHAPS represents 3-[(3-cholamidopropyl)dimethylammonio]propanesulfonic acid, ACES represents N-(2-acetamido)-2-aminoethanesulfonic acid, and MTT represents 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide.

TABLE 9 First reagent part Material solution for reagent part containing electron transfer substance (solvent is water) Ru coating 200 mM 0.2 ul Second reagent part Material solution for reagent part containing enzyme (solvent is water) Enzyme sucrose ACES coating enzymes conc. CHAPS monolaurate (pH 7.5) amount wild type 15 KU/ml 0.20% 0.05% 75 mM 0.1 ul 472D475H 15 KU/ml 0.20% 0.05% 75 mM 0.1 ul 472E475Y 15 KU/ml 0.20% 0.05% 75 mM 0.1 ul Third reagent part Material solution for reagent part containing color developer (solvent is water) MTT acrylamide methanol coating amount 60 mM 0.40% 50% 0.2 ul

An assay sample was supplied to the capillary of the aforementioned glucose sensor, and thereafter absorbance was repeatedly measured every 0.1 second to prepare a time course of absorbance. For each measurement of absorbance, the third reagent part (3) was irradiated with light along the direction of the height of the capillary, and light that transmitted through the glucose sensor was received upon the irradiation. The light irradiation was attained by irradiation with light of 630 nm using a light-emitting diode. The transmitted light was received with a photodiode.

As assay sample, blood added with glucose was used. Blood samples of which hematocrit was adjusted to 42% added with glucose at concentrations of 0, 100, 200 and 400 mg/dl were used to evaluate linearity of the glucose sensor. The results are shown in FIGS. 11 (wild type), 12 (472Glu475Tyr) and 13 (472Asp475His).

Further, blood samples of which hematocrit was adjusted to 42% and glucose concentration was adjusted to 45 mg/dl was further added with maltose at concentrations of 0, 100, 200 and 300 mg/dl, and used to evaluate influence of maltose. The results are shown in FIGS. 14 (wild type), 15 (472Glu475Tyr) and 16 (472Asp475His).

When maltose was added to the samples of 45 mg/dl of glucose, absorbance increased in a maltose concentration-dependent manner for the wild type, which suggested strong reaction with maltose. On the other hand, with the sensors using the mutant enzymes, the maltose concentration-dependent increase of the absorbance was suppressed, showing less influence of maltose. The results obtained by converting these data into apparent blood sugar elevation values are shown in FIG. 17. In the sensor using the wild type enzyme, a hypoglycemic level (45 mg/dl of glucose) is apparently shown as a normal value (122 mg/dl of glucose) due to contamination of maltose. On the other hand, when the sensor using the modified GDHs is used, the apparent blood sugar level does not elevate to the normal range even when the sample is contaminated with up to 300 mg/dl of maltose.

As clearly seen from the above results, in the glucose sensors using the mutant GDHs, reactivity to maltose was significantly decreased even though linearity was maintained to an extent comparable to that of the wild type. If these glucose sensors using the mutant GDHs are used, a hypoglycemic value (50 mg/dl or less) is not judged as a normal value or hyperglycemic level even at a maltose blood concentration of the upper limit (200 mg/dl) for administration at hospital or the like or higher, and thus safe therapeutic treatment can be conducted. Further, since GDHs do not react with dissolved oxygen as described above, accurate diagnosis and treatment of diabetic patients can be conducted by providing sensors using these mutant GDHs.

Example 8 Verification of Effect of Combination of Amino Acid Substitution at 472nd Position and Amino Acid Substitution at Position other than 475th Position

In a mutant GDH having 472Phe type substitution, substitution of phenylalanine was further introduced at positions in the vicinity of the 475th position (477th to 497th positions) and randomly selected positions far from the 475th position (53rd to 73rd positions).

Mutations were introduced in the same manner as in Example 2 by using pTrc99Aγαβ expressing a mutant GDH containing substitution of phenylalanine at the 472nd position. The sequences of the forward primers used for the introduction of mutations are shown in Tables 10 and 11. The sequences of the reverse primers were completely complementary strands of the forward primers.

TABLE 10 Mutation SEQ ID NO: I477F 19 T478F 20 G479F 21 S480F 22 T481F 23 I482F 24 M483F 25 G484F 26 A485F 27 D486F 28 A487F 29 R488F 30 D489F 31 S490F 32 V491F 33 V492F 34 D493F 35 K494F 36 D495F 37 C496F 38 R497F 39

TABLE 11 Mutation SEQ ID NO: R53F 40 N54F 41 Q55F 42 P56F 43 D57F 44 K58F 45 M59F 46 D60F 47 M62F 48 A63F 49 P64F 50 Y65F 51 P66F 52 S67F 53 S68F 54 P69F 55 W70F 56 A71F 57 P72F 58 H73F 59

The results are shown in Tables 12 and 13. As clearly seen from these results, with combinations of amino acid substitution of 472Phe and substitution at positions other than the 475th position, activity was lost, no change occurred, or only an effect of increasing the reactivity to maltose was observed, and thus it was confirmed that the improving effect was not necessarily obtained by introducing mutations at any arbitrary positions.

TABLE 12 10 mM 10 mM Mal/Glu mutated substituting Glucose Maltose reaction site amino acid U/ml U/ml ratio 472F None 6.79 0.81   12% 472F+ 475 F(Phe) 0.75 0.07  8.7% 472F+ 477 F(Phe) 0.11 0.16 inactive 472F+ 478 F(Phe) 0.12 0.12 inactive 472F+ 479 F(Phe) 0.21 0.21 inactive 472F+ 480 F(Phe) 0.26 0.30 inactive 472F+ 481 F(Phe) 0.10 0.08 inactive 472F+ 482 F(Phe) 0.06 0.08 inactive 472F+ 483 F(Phe) 4.32 0.68 15.6% 472F+ 484 F(Phe) 0.10 0.10 inactive 472F+ 485 F(Phe) 0.18 0.24 inactive 472F+ 486 F(Phe) 1.26 0.40 32.0% 472F+ 487 F(Phe) 0.22 0.23 inactive 472F+ 488 F(Phe) 2.85 0.65 22.9% 472F+ 489 F(Phe) 1.81 0.56 31.2% 472F+ 490 F(Phe) 0.18 0.19 inactive 472F+ 491 F(Phe) 0.23 0.23 inactive 472F+ 492 F(Phe) 0.19 0.24 inactive 472F+ 493 F(Phe) 0.15 0.15 inactive 472F+ 494 F(Phe) 1.15 0.29 25.0% 472F+ 495 F(Phe) 0.29 0.23 inactive 472F+ 496 F(Phe) 0.16 0.18 inactive 472F+ 497 F(Phe) 0.14 0.16 inactive

TABLE 13 10 mM 10 mM Mal/Glu mutated substituting Glucose Maltose reaction site amino acid U/ml U/ml ratio 472F None 6.79 0.81 11. 9% 472F+ 475 F(Phe) 0.75 0.07 8.7% 472F+ 53 F(Phe) 3.44 0.48 13.8% 472F+ 54 F(Phe) 3.00 0.54 18.2% 472F+ 55 F(Phe) 3.81 0.72 18.8% 472F+ 56 F(Phe) 4.89 0.57 11.7% 472F+ 57 F(Phe) 2.41 0.41 17.2% 472F+ 58 F(Phe) 3.33 0.45 13.5% 472F+ 59 F(Phe) 4.07 0.58 14.2% 472F+ 60 F(Phe) 1.55 0.37 23.7% 472F+ 62 F(Phe) 1.31 0.26 19.9% 472F+ 63 F(Phe) 2.91 0.44 15.0% 472F+ 64 F(Phe) 0.54 0.28 51.4% 472F+ 65 F(Phe) 5.52 0.76 13.8% 472F+ 66 F(Phe) 1.63 0.35 21.8% 472F+ 67 F(Phe) 3.91 0.48 12.3% 472F+ 68 F(Phe) 4.32 0.86 19.8% 472F+ 69 F(Phe) 4.79 0.82 17.1% 472F+ 70 F(Phe) 5.34 0.64 12.0% 472F+ 71 F(Phe) 1.26 0.28 22.5% 472F+ 72 F(Phe) 3.65 0.50 13.8% 472F+ 73 F(Phe) 1.20 0.26 21.3%

INDUSTRIAL APPLICABILITY

The mutant GDH of the present invention has improved substrate specificity to glucose and can be suitably used for measurement of glucose using a glucose sensor or the like. 

1. A mutant glucose dehydrogenase exhibiting improved substrate specificity to glucose, which is a protein having the amino acid sequence of SEQ ID NO: 13 or an amino acid sequence of SEQ ID NO: 13 including substitution, deletion, insertion or addition of one or more amino acid residues at position other than the positions listed below and having a glucose dehydrogenase activity, and having any of the amino acid substitution mutations listed below (numerals represent a position in the amino acid sequence, the amino acid residues represent an amino acid residue after substitution at the position, and “+” means that two amino acid substitutions are simultaneously included): (A) 472Arg, 472Asn, 472Asp, 472Cys, 472Glu, 472Gly, 472His, 4721le, 472Leu, 472Met, 472Phe, 472Pro, 472Ser, 472Trp, 472Tyr, 472Val, (B) 475Asp, 475Cys, 475Glu, 475Gly, 475His, 475Met, 475Phe, 475Ser, 475Tyr, 475Val, (C) 472Arg+475(Asp, Glu, Gly, His, Phe, Ser, Tyr), 472Asn+475(Asp, Gly, His, Phe, Ser, Tyr), 472Asp+475(H is, Phe, Ser, Val), 472Cys+475(Asp, Gly, His, Phe, Ser), 472Glu+475(Asp, Glu, Gly, His, Phe, Ser, Tyr), 472Gly+475(Asp, Cys, Gly, Met, Phe, Ser, Tyr), 472His+475(Cys, Glu, His, Met, Phe, Ser, Tyr), 472Ile+475(Asp, Cys, Glu, Gly, His, Met, Phe, Ser, Tyr), 472Leu+475(Asp, Gly, His, Phe, Ser, Tyr), 472Met+475(Asp, Gly, His, Phe, Ser), 472Phe+475(Asp, Glu, Gly, His, Met, Phe, Ser, Tyr), 472Pro+475His 472Ser+475(Asp, Glu, Gly, His, Phe, Ser), 472Trp+475(H is, Phe, Ser), 472Tyr+475(Asp, His, Phe, Ser), 472Val+475(Asp, Glu, Gly, His, Phe, Ser).
 2. The mutant glucose dehydrogenase according to claim 1, which has the amino acid sequence of SEQ ID NO: 13 provided that it includes any of the amino acid substitution mutations listed in the aforementioned (A) to (C).
 3. The mutant glucose dehydrogenase according to claim 1, which has an amino acid substitution mutation selected from the following mutations: (D) 472Arg, 472Asn, 472Asp, 472Glu, 472Gly, 472Phe, 472Pro, (E) 475Asp, 475Cys, 475Glu, 475Gly, 475Met, 475Phe (F) 472Arg+475(Asp, Gly, His, Phe), 472Asn+475(Gly, His, Phe, Tyr), 472Asp+475(H is, Ser), 472Cys+475(Gly, His, Phe), 472Glu+475(Glu, His, Phe, Tyr), 472Gly+475(Asp, Phe, Tyr), 472His+475(H is, Ser), 472Ile+475(Asp, Glu, Gly, His, Ser), 472Leu+475(Gly, His, Phe, Tyr), 472Met+475(Asp, Gly, His, Phe), 472Phe+475(Asp, Glu, Gly, His, Phe, Ser, Tyr), 472Ser+475(Glu, Gly, His, Phe), 472Trp+475(H is, Phe), 472Tyr+475His, 472Val+475(Asp, Glu, Gly, His, Phe).
 4. A glucose dehydrogenase, which is a protein having the amino acid sequence of SEQ ID NO: 13 or an amino acid sequence of SEQ ID NO: 13 including substitution, deletion, insertion or addition of one or more amino acid residues at position other than the positions listed below and having a glucose dehydrogenase activity, and wherein: (i) at least either the arginine residue at position 472 or the asparagine residue at position 475 in the amino acid sequence of SEQ ID NO: 13 is replaced with another amino acid residue, and (ii) a ratio of specific activity for glucose and specific activity for maltose ((reactivity to maltose/reactivity to glucose)×100) of the glucose dehydrogenase introduced with the mutation is reduced by 10% or more compared with that of a glucose dehydrogenase not introduced with the mutation.
 5. A mutant glucose dehydrogenase complex comprising at least the mutant glucose dehydrogenase according to claim 1 and an electron transfer subunit.
 6. A DNA coding for the mutant glucose dehydrogenase according to claim
 1. 7. A microorganism comprising the DNA according to claim 6, optionally in combination with an electron transfer subunit.
 8. A glucose assay kit comprising the mutant glucose dehydrogenase according to claim 1, optionally in combination with an electron transfer subunit, or a microorganism comprising a DNA coding for the mutant glucose dehydrogenase according to claim
 1. 9. A glucose sensor comprising the mutant glucose dehydrogenase according to claim 1, optionally in combination with an electron transfer subunit, or a microorganism comprising a DNA coding for the mutant glucose dehydrogenase according to claim
 1. 10. A mutant glucose dehydrogenase complex comprising at least the mutant glucose dehydrogenase according to claim 4 and an electron transfer subunit.
 11. A DNA coding for the mutant glucose dehydrogenase according to claim
 4. 12. A microorganism comprising the DNA according to claim 11, optionally in combination with an electron transfer subunit.
 13. A glucose assay kit comprising the mutant glucose dehydrogenase according to claim 4, optionally in combination with an electron transfer subunit, or a microorganism comprising a DNA coding for the mutant glucose dehydrogenase according to claim
 4. 14. A glucose sensor comprising the mutant glucose dehydrogenase according to claim 4, optionally in combination with an electron transfer subunit, or a microorganism comprising a DNA coding for the mutant glucose dehydrogenase according to claim
 4. 15. A mutant glucose dehydrogenase complex comprising at least the mutant glucose dehydrogenase according to claim 2 and an electron transfer subunit.
 16. A DNA coding for the mutant glucose dehydrogenase according to claim
 2. 17. A microorganism comprising the DNA according to claim 16, optionally in combination with an electron transfer subunit.
 18. A glucose assay kit or glucose sensor comprising the mutant glucose dehydrogenase according to claim 2, optionally in combination with an electron transfer subunit, or a microorganism comprising a DNA coding for the mutant glucose dehydrogenase according to claim
 2. 19. A mutant glucose dehydrogenase complex comprising at least the mutant glucose dehydrogenase according to claim 3 and an electron transfer subunit.
 20. A DNA coding for the mutant glucose dehydrogenase according to claim
 3. 21. A microorganism comprising the DNA according to claim 20, optionally in combination with an electron transfer subunit.
 22. A glucose assay kit or glucose sensor comprising the mutant glucose dehydrogenase according to claim 3, optionally in combination with an electron transfer subunit, or a microorganism comprising a DNA coding for the mutant glucose dehydrogenase according to claim
 3. 